List of variants in gene DDX3X reported as not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 20

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HGVS	dbSNP	gnomAD frequency
NM_001356.5(DDX3X):c.236G>A (p.Arg79Lys)	rs1064795656	0.00002
NM_001356.5(DDX3X):c.1052G>A (p.Arg351Gln)	rs1057518707
NM_001356.5(DDX3X):c.1084C>T (p.Arg362Cys)	rs797045026
NM_001356.5(DDX3X):c.1126C>T (p.Arg376Cys)	rs796052231
NM_001356.5(DDX3X):c.1127G>A (p.Arg376His)	rs2063908570
NM_001356.5(DDX3X):c.1168C>T (p.Gln390Ter)
NM_001356.5(DDX3X):c.121C>T (p.Pro41Ser)	rs1064793796
NM_001356.5(DDX3X):c.1399G>T (p.Ala467Ser)	rs2147358490
NM_001356.5(DDX3X):c.1486G>A (p.Val496Met)	rs1555954154
NM_001356.5(DDX3X):c.1535_1536del (p.His512fs)	rs796052230
NM_001356.5(DDX3X):c.1702C>T (p.Pro568Ser)	rs2147360044
NM_001356.5(DDX3X):c.1710G>A (p.Trp570Ter)	rs1555954388
NM_001356.5(DDX3X):c.443+3A>T	rs2147350644
NM_001356.5(DDX3X):c.538G>T (p.Glu180Ter)
NM_001356.5(DDX3X):c.629C>T (p.Ala210Val)
NM_001356.5(DDX3X):c.641_643delinsCC (p.Ile214fs)	rs1131691571
NM_001356.5(DDX3X):c.744C>T (p.Gly248=)	rs1569238002
NM_001356.5(DDX3X):c.862A>G (p.Lys288Glu)	rs1064796820
NM_001356.5(DDX3X):c.898G>T (p.Val300Phe)	rs2147353947
NM_001356.5(DDX3X):c.977G>A (p.Arg326His)	rs797045025

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